Congenital hypofibrinogenemia.
dc.contributor.author | Awasthy, Neeraj | en_US |
dc.contributor.author | Aggarwal, K C | en_US |
dc.contributor.author | Gupta, H | en_US |
dc.contributor.author | Saluja, S | en_US |
dc.date.accessioned | 2004-02-09 | en_US |
dc.date.accessioned | 2009-05-27T06:14:58Z | |
dc.date.available | 2004-02-09 | en_US |
dc.date.available | 2009-05-27T06:14:58Z | |
dc.date.issued | 2004-02-09 | en_US |
dc.description.abstract | Congenital afibrinogenemia/hypofibrinogenemia is an extremely rare coagulation disorder. We describe a case of congenital hypofibrinogenemia in a 6-year female child, who presented with recurrent ecchymotic spots with no frank bleeding. | en_US |
dc.description.affiliation | Department of Pediatrics, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi 110 029, India. | en_US |
dc.identifier.citation | Awasthy N, Aggarwal KC, Gupta H, Saluja S. Congenital hypofibrinogenemia. Indian Pediatrics. 2004 Feb; 41(2): 185-7 | en_US |
dc.identifier.uri | https://imsear.searo.who.int/handle/123456789/15713 | |
dc.language.iso | eng | en_US |
dc.source.uri | https://indianpediatrics.net | en_US |
dc.subject.mesh | Afibrinogenemia --complications | en_US |
dc.subject.mesh | Blood Coagulation Disorders --congenital | en_US |
dc.subject.mesh | Child | en_US |
dc.subject.mesh | Combined Modality Therapy | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Hemorrhage --etiology | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | India | en_US |
dc.subject.mesh | Prognosis | en_US |
dc.subject.mesh | Recurrence | en_US |
dc.subject.mesh | Severity of Illness Index | en_US |
dc.title | Congenital hypofibrinogenemia. | en_US |
dc.type | Case Reports | en_US |
dc.type | Journal Article | en_US |
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